Canonical Allele Identifier: CA529464714

Gene: COQ8A

Linked Data

• dbSNP Id: rs1446557017
• gnomAD v2: 1-227171946-T-C
• MyVariant Identifiers: chr1:g.227171946T>C (hg19) ; chr1:g.226984245T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226984245T>C , CM000663.2:g.226984245T>C	GRCh38
NC_000001.10:g.227171946T>C , CM000663.1:g.227171946T>C	GRCh37
NC_000001.9:g.225238569T>C	NCBI36
NG_012825.1:g.49009T>C
NG_012825.2:g.91710T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366777.4:c.1398+10T>C MANE Select	ENSP00000355739.3:n.1398+10T>C
ENST00000366779.6:c.*6125+10T>C	ENSP00000355741.2:n.*6125+10T>C
ENST00000366777.3:c.1398+10T>C	ENSP00000355739.3:n.1398+10T>C
ENST00000366778.5:c.1242+10T>C	ENSP00000355740.1:n.1242+10T>C
ENST00000366779.5:c.1398+10T>C	ENSP00000355741.1:n.1398+10T>C
ENST00000478406.5:n.2260+10T>C
ENST00000479852.1:n.585+10T>C
ENST00000485462.5:n.788+10T>C
NM_020247.4:c.1398+10T>C	NP_064632.2:n.1398+10T>C
XM_005273201.1:c.1398+10T>C	XP_005273258.1:n.1398+10T>C
XM_011544238.1:c.1398+10T>C	XP_011542540.1:n.1398+10T>C
XM_011544239.1:c.1398+10T>C	XP_011542541.1:n.1398+10T>C
XM_011544240.1:c.1398+10T>C	XP_011542542.1:n.1398+10T>C
XM_011544241.1:c.1398+10T>C	XP_011542543.1:n.1398+10T>C
XM_011544239.2:c.1398+10T>C	XP_011542541.1:n.1398+10T>C
XM_011544241.2:c.1398+10T>C	XP_011542543.1:n.1398+10T>C
XM_017001852.1:c.1398+10T>C	XP_016857341.1:n.1398+10T>C
XM_024448517.1:c.1398+10T>C	XP_024304285.1:n.1398+10T>C
XM_024448518.1:c.1398+10T>C	XP_024304286.1:n.1398+10T>C
NM_020247.5:c.1398+10T>C MANE Select	NP_064632.2:n.1398+10T>C